Linked Data
ClinVar Variation Id:
480106
dbSNP Id:
rs778799019
ExAC:
17:29686023 C / T
gnomAD v2:
17-29686023-C-T
gnomAD v3:
17-31359005-C-T
gnomAD v4:
17-31359005-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.31359005C>T , CM000679.2:g.31359005C>T | GRCh38 |
| NC_000017.10:g.29686023C>T , CM000679.1:g.29686023C>T | GRCh37 |
| NC_000017.9:g.26710149C>T | NCBI36 |
| NG_009018.1:g.269029C>T , LRG_214:g.269029C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696138.1:c.8132C>T | ENSP00000512431.1:p.Pro2711Leu | |
| ENST00000684826.1:c.2714C>T | ENSP00000509994.1:p.Pro905Leu | |
| ENST00000687027.1:c.2306C>T | ENSP00000508715.1:p.Pro769Leu | |
| ENST00000689464.1:c.1200C>T | ||
| ENST00000691014.1:c.8180C>T | ENSP00000510595.1:p.Pro2727Leu | |
| ENST00000693617.1:c.2714C>T | ENSP00000510031.1:p.Pro905Leu | |
| ENST00000358273.9:c.8150C>T MANE Select | ENSP00000351015.4:p.Pro2717Leu | |
| ENST00000356175.7:c.8087C>T | ENSP00000348498.3:p.Pro2696Leu | |
| ENST00000358273.8:c.8150C>T | ENSP00000351015.4:p.Pro2717Leu | |
| ENST00000456735.6:c.7085C>T | ENSP00000389907.2:p.Pro2362Leu | |
| ENST00000468273.1:c.112C>T | ||
| ENST00000471572.6:c.1533C>T | ||
| ENST00000577967.1:n.3202C>T | ||
| ENST00000579081.5:c.8286C>T | ENSP00000462408.1:n.8286C>T | |
| ENST00000581790.5:c.1135C>T | ||
| NM_000267.3:c.8087C>T , LRG_214t1:c.8087C>T | NP_000258.1:p.Pro2696Leu | |
| NM_001042492.2:c.8150C>T , LRG_214t2:c.8150C>T | NP_001035957.1:p.Pro2717Leu | |
| XM_005257983.1:c.8150C>T | XP_005258040.1:p.Pro2717Leu | |
| XM_005257984.1:c.8087C>T | XP_005258041.1:p.Pro2696Leu | |
| XM_006721922.1:c.8180C>T | XP_006721985.1:p.Pro2727Leu | |
| XM_006721923.2:c.8141C>T | XP_006721986.1:p.Pro2714Leu | |
| XM_006721924.1:c.8180C>T | XP_006721987.1:p.Pro2727Leu | |
| XM_006721925.1:c.8117C>T | XP_006721988.1:p.Pro2706Leu | |
| XM_006721926.2:c.8180C>T | XP_006721989.1:p.Pro2727Leu | |
| XM_006721927.1:c.8180C>T | XP_006721990.1:p.Pro2727Leu | |
| XM_011524852.1:c.8177C>T | XP_011523154.1:p.Pro2726Leu | |
| XM_011524853.1:c.8141C>T | XP_011523155.1:p.Pro2714Leu | |
| XM_011524854.1:c.8141C>T | XP_011523156.1:p.Pro2714Leu | |
| XM_011524855.1:c.8141C>T | XP_011523157.1:p.Pro2714Leu | |
| XM_011524856.1:c.8141C>T | XP_011523158.1:p.Pro2714Leu | |
| XM_011524857.1:c.8057C>T | XP_011523159.1:p.Pro2686Leu | |
| NM_001042492.3:c.8150C>T MANE Select | NP_001035957.1:p.Pro2717Leu |